The following data is part of a premarket notification filed by Ditron Precision Ltd with the FDA for Dental Implants And Abutments.
Device ID | K161497 |
510k Number | K161497 |
Device Name: | Dental Implants And Abutments |
Classification | Implant, Endosseous, Root-form |
Applicant | Ditron Precision Ltd Haofe 2 St., P.O Box 5010 Netanya, IL 78150 |
Contact | Moshe Orlev |
Correspondent | Tali Hazan Talmed Ltd Ramot Naftali, M.P Upper Galillee Ramot Naftali, IL 13830000 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-06-01 |
Decision Date | 2016-10-28 |
Summary: | summary |